trans-tert-Butyl 3,4-bis(hydroxymethyl)pyrrolidine-1-carboxylate

trans-tert-Butyl 3,4-bis(hydroxymethyl)pyrrolidine-1-carboxylate

trans-1-(benzyloxycarbonyl)-4-methoxypyrrolidine-3-carboxylic acid

trans-1-(benzyloxycarbonyl)-4-methoxypyrrolidine-3-carboxylic acid

(S)-1-methylpyrrolidine-2-carboxamide

$250.00
CAS No.: 94391-71-6
Catalog No.: 193048
Purity: 95%
MF: C6H12N2O
MW: 128.175
Storage: 2-8 degree Celsius
SMILES: CN1[C@@H](CCC1)C(=O)N
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193048
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(S)-1-methylpyrrolidine-2-carboxamide; CAS No.: 94391-71-6; (S)-1-methylpyrrolidine-2-carboxamide. PROPERTIES: This compound appears as a white to off-white crystalline solid with molecular formula C6H12N2O and a molecular weight of 128.17 g/mol. It exhibits a melting point in the range of 132-136 C and demonstrates moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to oxidation and should be stored under inert atmosphere. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as (S)-1-methylpyrrolidine-2-carboxamide may cause skin irritation. The amide group requires careful handling in strongly basic environments. APPLICATIONS: In medicinal chemistry, (S)-1-methylpyrrolidine-2-carboxamide serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its methyl substituent enables improved solubility in biological systems for enhanced bioavailability. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The pyrrolidine ring system also facilitates coordination with metal ions, making it valuable for creating coordination polymers in materials science applications, as evidenced by structural chemistry publications.

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